Crystal structure of the adenosine A2Areceptor bound to an antagonist reveals a potential allosteric pocket

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Unprecedented Therapeutic Potential with a Combination of A2A/NR2B Receptor Antagonists as Observed in the 6-OHDA Lesioned Rat Model of Parkinson's Disease

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Discovery of 1,2,4-Triazine Derivatives as Adenosine A2A Antagonists using Structure Based Drug Design

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Structural Basis for Allosteric Regulation of GPCRs by Sodium Ions

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Adenosine A2A Receptor Antagonists and Parkinson’s Disease

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Structure of an Agonist-Bound Human A2A Adenosine Receptor

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Structure of the Adenosine A2A Receptor in Complex with ZM241385 and the Xanthines XAC and Caffeine

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The 2.6 Angstrom Crystal Structure of a Human A2A Adenosine Receptor Bound to an Antagonist

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